Hematology Center, Beijing Key Laboratory of Pediatric Hematology Oncology, National Key Discipline of Pediatrics (Capital Medical University), Key Laboratory of Major Disease in Children, Ministry of Education, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Hematologic Disease Laboratory, Beijing Pediatric Research Institute, Hematology Center, Beijing Key Laboratory of Pediatric Hematology Oncology, National Key Discipline of Pediatrics (Capital Medical University), Key Laboratory of Major Disease in Children, Ministry of Education, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Pediatr Blood Cancer. 2022 Aug;69(8):e29712. doi: 10.1002/pbc.29712. Epub 2022 Apr 20.
To analyze the clinical significance of soluble CD25 (sCD25) levels in cerebrospinal fluid (CSF) in pediatric hemophagocytic lymphohistiocytosis (HLH) with central nervous system (CNS) involvement.
All patients diagnosed with HLH admitted to Beijing Children's Hospital, Capital Medical University between January 1, 2017 and October 31, 2021 who received a measurement of their HLH-related parameters and CSF sCD25 levels at admission were enrolled in this study.
CSF sCD25 levels in patients with primary HLH were higher than those in patients with Epstein-Barr virus infection-associated HLH, and the median level was 444 pg/ml. The difference in CSF sCD25 levels between the non-CNS group and the CNS group was statistically significant (591 [259-33,643] pg/ml vs. 123 (36-437) pg/ml, p < .001). The best cutoff value of CSF sCD25 was 273.5 pg/ml (AUC = 0.987, 95% CI: 0.972-1.000), with sensitivity, specificity, positive predictive values, and negative predictive values of 96.4%, 92.8%, 81.8%, and 98.7%, respectively. CSF sCD25 in the severe CNS involvement group was significantly higher than that in the nonsevere CNS involvement group (p = .014). The 3-year overall survival (OS) of patients with high CSF sCD25 levels was lower than that of patients with low CSF sCD25 levels(71.6% ± 8.1% vs. 93.3% ± 2.9%, hazard ratio [HR] = 3.637, p = .003).
Increased CSF sCD25 levels in active disease can predict CNS-HLH. Primary HLH has a higher CSF sCD25 level than Epstein-Barr virus infection-associated HLH. Patients who are diagnosed with CNS-HLH with CSF sCD25 levels higher than 273.5 pg/ml are more likely to develop severe CNS involvement, suggesting a poor prognosis.
分析可溶性 CD25(sCD25)在伴有中枢神经系统(CNS)受累的儿科噬血细胞性淋巴组织细胞增多症(HLH)患者脑脊液(CSF)中的临床意义。
本研究纳入了 2017 年 1 月 1 日至 2021 年 10 月 31 日期间首都医科大学附属北京儿童医院收治的所有初诊为 HLH 且入院时检测了 HLH 相关参数和 CSF sCD25 水平的患者。
原发性 HLH 患者的 CSF sCD25 水平高于 EBV 感染相关性 HLH 患者,中位数为 444pg/ml。非 CNS 组和 CNS 组的 CSF sCD25 水平差异有统计学意义(591[259-33643]pg/ml 比 123[36-437]pg/ml,p<0.001)。CSF sCD25 的最佳截断值为 273.5pg/ml(AUC=0.987,95%CI:0.972-1.000),灵敏度、特异度、阳性预测值和阴性预测值分别为 96.4%、92.8%、81.8%和 98.7%。重度 CNS 受累组的 CSF sCD25 水平明显高于非重度 CNS 受累组(p=0.014)。CSF sCD25 水平较高的患者 3 年总生存率(OS)低于 CSF sCD25 水平较低的患者(71.6%±8.1%比 93.3%±2.9%,HR=3.637,p=0.003)。
活动期 CSF sCD25 水平升高可预测 CNS-HLH。原发性 HLH 的 CSF sCD25 水平高于 EBV 感染相关性 HLH。CSF sCD25 水平高于 273.5pg/ml 的 CNS-HLH 患者更易发生重度 CNS 受累,提示预后不良。